UBE2F ubiquitin conjugating enzyme E2 F (putative)
Information
- Symbol
- UBE2F
- Type
- protein-coding
- Description
- ubiquitin conjugating enzyme E2 F (putative)
- Entrez Gene ID
- 140739
- Genome
- hg19
- Position
- chr2:238,875,656-238,951,423
- Genome
- hg38
- Position
- chr2:237,967,014-238,042,782
- MIM
- 617700 OMIM
- HGNC
- HGNC:12480 HGNC
- Ensembl
- ENSG00000184182 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 12 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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12 |
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0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | NCE2 |
MIM | 617700 OMIM |
HGNC | HGNC:12480 HGNC |
Ensembl | ENSG00000184182 Ensembl |
AllianceGenome | HGNC:12480 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000272930.9 | hg38 | chr2 | 237,967,014 | 238,042,782 | 75,769 |
ENST00000414443.5 | hg38 | chr2 | 237,966,955 | 238,042,782 | 75,828 |
ENST00000409332.5 | hg38 | chr2 | 237,967,082 | 238,041,917 | 74,836 |
ENST00000409953.5 | hg38 | chr2 | 237,967,081 | 238,041,770 | 74,690 |
ENST00000409633.5 | hg38 | chr2 | 237,967,014 | 238,041,545 | 74,532 |
ENST00000612130.4 | hg38 | chr2 | 237,968,793 | 238,042,782 | 73,990 |
ENST00000272930.9 | hg19 | chr2 | 238,875,656 | 238,951,423 | 75,768 |
ENST00000409332.5 | hg19 | chr2 | 238,875,724 | 238,950,558 | 74,835 |
ENST00000409633.5 | hg19 | chr2 | 238,875,656 | 238,950,186 | 74,531 |
ENST00000409953.5 | hg19 | chr2 | 238,875,723 | 238,950,411 | 74,689 |
ENST00000414443.5 | hg19 | chr2 | 238,875,597 | 238,951,423 | 75,827 |
ENST00000612130.4 | hg19 | chr2 | 238,877,435 | 238,951,423 | 73,989 |
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